Surgical stapling device including a buttress retention assembly

ABSTRACT

A buttress assembly for use with a surgical stapling device includes a buttress material and a loading assembly. The buttress material includes proximal and distal portions. The proximal portion defines proximal bores and a proximal slot. The distal portion defines distal bores and a distal slot. The loading assembly includes proximal and distal wings and proximal and distal cups. Each of the proximal wings includes a proximal peg configured to be received in a corresponding one of the proximal bores of the buttress material. Each of the distal wings includes a distal peg configured to be received in a corresponding one of the distal bores of the buttress material. When the proximal pegs are received in the proximal bores, the proximal cup is in registration with the proximal slot, and when the distal pegs are received in the distal bores, the distal cup is in registration with the distal slot.

FIELD

The disclosure relates to surgical stapling devices, and more particularly, to assemblies and methods for detachably securing or retaining a staple line buttress assembly to a surgical stapling device.

BACKGROUND

Surgical stapling devices are employed by surgeons to sequentially or simultaneously apply one or more rows of fasteners, e.g., staples or two-part fasteners, to body tissue for the purpose of joining segments of body tissue together. When stapling relatively thin or fragile tissues, it is important to effectively seal the staple line against air or fluid leakage. Additionally, it is often necessary to reinforce the staple line against the tissue to inhibit tears in the tissue or pulling of the staples through the tissue. One method of inhibiting tears or pull through involves the placement of a biocompatible reinforcing material or “buttress” material between the staples and the underlying tissue. In this method, a layer of buttress assembly is placed against the tissue and the tissue is stapled in a conventional manner.

Accordingly, new systems and methods that enable easy and efficient attachment and removal of a buttress assembly to a surgical stapling device would be desirable.

SUMMARY

A surgical kit in accordance with the disclosure includes a surgical stapling device, a buttress material, and a loading assembly. The surgical stapling device includes a tool assembly including first and second jaw members that are transitionable between open and closed configurations. The first jaw member supports a staple cartridge that includes a retention assembly and defines proximal and distal slots. The retention assembly includes a proximal hook disposed within the proximal slot of the staple cartridge and a distal hook disposed within the distal slot of the staple cartridge. The buttress material includes an elongate body having proximal and distal portions, proximal protrusions extending laterally outwards from the proximal portion of the elongate body, and distal protrusions extending laterally outwards from the distal portion of the elongate body. The proximal protrusions define respective proximal bores. The distal protrusions define respective distal bores. The buttress material define a proximal slot interposed between the proximal bores and a distal slot interposed between the distal bores. The loading assembly includes proximal wings that are laterally spaced apart, distal wings that are laterally spaced apart, a proximal cup configured to receive a portion of the proximal hook of the staple cartridge and engage a first portion of the buttress material to position the first portion of the buttress material in the proximal slot of the staple cartridge to be releasably secured to the proximal hook, and a distal cup configured to receive a portion of the distal hook of the staple cartridge and engage a second portion of the buttress material to position the second portion of the buttress material in the distal slot of the staple cartridge to be releasably secured to the distal hook. Each of the proximal wings includes a proximal peg configured to be received through a corresponding one of the proximal bores of the buttress material. Each of the distal wings includes a distal peg configured to be received through a corresponding one of the distal bores of the buttress material.

In an aspect, the loading assembly may further include a contact pad disposed about a portion of one of the proximal and distal pegs of the loading assembly.

In another aspect, the proximal portion of the loading assembly may define cutouts on lateral sides of the loading assembly.

In yet another aspect, the staple cartridge may include tabs received in the respective cutouts of the loading assignment.

In yet another aspect, the distal portion of the loading assembly may have a guide and the staple cartridge may define a knife channel. The guide may be configured to be received in the knife channel of the staple cartridge.

In still yet another aspect, the proximal and distal pegs of the loading assembly may be configured to support the buttress material by friction or interference fit.

In still yet another aspect, the proximal or distal cups may have a non-circular cross-section.

In still yet another aspect, the proximal cup may be interposed between the proximal pegs.

In an aspect, the proximal or distal hooks may be formed of an elastic material to enable axial flexing of the proximal or distal hooks.

In another aspect, the buttress material may be formed of an elastic material that is placed in tension when the buttress material is secured to the staple cartridge.

In yet another aspect, the proximal slot of the buttress material may be in registration with the proximal cup when the buttress material is mounted on the loading assembly.

In accordance with another aspect of the disclosure, a buttress assembly for use with a surgical stapling device includes a buttress material and a loading assembly. The buttress material includes proximal and distal portions. The proximal portion defines proximal bores laterally spaced apart and a proximal slot interposed between the proximal bores. The distal portion defines distal bores laterally spaced apart and a distal slot interposed between the distal bores. The loading assembly includes proximal wings that are laterally spaced apart, distal wings that are laterally spaced apart, a proximal cup interposed between the proximal pegs and configured to engage a first portion of the buttress material, and a distal cup interposed between the distal pegs and configured to engage a second portion of the buttress material. Each of the proximal wings includes a proximal peg configured to be received in a corresponding one of the proximal bores of the buttress material. Each of the distal wings includes a distal peg configured to be received in a corresponding one of the distal bores of the buttress material. When the proximal pegs of the loading assembly are received in the proximal bores of the buttress material, the proximal cup is in registration with the proximal slot of the buttress material, and when the distal pegs of the loading assembly are received in the distal bores of the buttress material, the distal cup is in registration with the distal slot of the buttress material.

In an aspect, the loading assembly may have opposing cutouts on lateral sides of the loading assembly.

In another aspect, a proximal end of the buttress material may have a notch.

In yet another aspect, the distal portion of the loading assembly may have a guide extending along a length of the loading assembly.

In still yet another aspect, the guide of the loading assembly may be distal of the distal pegs.

In still yet another aspect, the loading assembly may be symmetric about a central longitudinal axis.

In still yet another aspect, the buttress material may be bioabsorbable.

BRIEF DESCRIPTION OF THE DRAWINGS

The above and other aspects and features of this disclosure will become more apparent in view of the following detailed description when taken in conjunction with the accompanying drawings wherein like reference numerals identify similar or identical elements.

FIG. 1 is a perspective view of a surgical stapling device in accordance with the disclosure;

FIG. 2 is an enlarged view of the indicated area of detail of FIG. 1 ;

FIG. 3 is a perspective view of a tool assembly of FIG. 2 , illustrating a staple cartridge separated from a jaw member of the tool assembly;

FIG. 4 is an enlarged view of the indicated area of detail of FIG. 3 ;

FIG. 5 is an enlarged view of the indicated area of detail of FIG. 3 ;

FIG. 6 is a perspective view of a buttress assembly and the staple cartridge of FIG. 3 ;

FIG. 7 is a side cross-sectional view of the staple cartridge of FIG. 6 taken along section line 7-7 of FIG. 6 ;

FIG. 8 is an enlarged view of the indicated area of detail of FIG. 7 ;

FIG. 9 is an enlarged view of the indicated area of detail of FIG. 7 ;

FIG. 10 is a perspective view of a loading assembly of FIG. 6 ;

FIG. 11 is a perspective view of the loading assembly of FIG. 10 and a buttress material mounted on the loading assembly;

FIG. 12 is a perspective view of the loading assembly and the staple cartridge of FIG. 11 , illustrating mounting of the buttress material on the staple cartridge;

FIG. 13 is a partial side cross-sectional view taken along section line 13-13 of FIG. 12 ; and

FIG. 14 is a partial side cross-sectional view of the staple cartridge, the buttress material, and the loading assembly, illustrating releasable mounting of the buttress material on the staple cartridge.

DETAILED DESCRIPTION

The surgical stapling device including a buttress retention assembly disclosed herein is described in detail with reference to the drawings, in which like reference numerals designate identical or corresponding elements in each of the several views. As used herein, the term “distal” refers to the portion of the device that is being described which is farther from a user in a conventional use of the surgical stapling device, while the term “proximal” refers to the portion of the device that is being described which is closer to a user in a conventional use of the surgical stapling device. In addition, the terms parallel and perpendicular are understood to include relative configurations that are substantially parallel and substantially perpendicular up to about + or −10 degrees from true parallel and true perpendicular. Further, to the extent consistent, any or all of the aspects detailed herein may be used in conjunction with any or all of the other aspects detailed herein.

With reference to FIGS. 1 and 2 , there is provided a surgical stapling device 200 for use in stapling tissue and applying a layer of buttress material 310 between staples and underlying tissue. The layer of buttress material 310 is configured to reinforce and seal staple lines applied to tissue by the surgical stapling device 200. The surgical stapling device 200 generally includes a handle 202 and an elongate tubular member 204 extending distally from the handle 202. A reload 106 is removably coupled to a distal end 105 of the elongate tubular member 204. The reload 106 includes a shaft portion 109 and a tool assembly 107 supported on the shaft portion 109. The tool assembly 107 includes first jaw member 108 and a second jaw member 110 that is movable in relation to the first jaw member 108 between an open configuration for positioning tissue between the first and second jaw members 108, 110 and a closed configuration for clamping tissue between the first and second jaw members 108, 110 and subsequently stapling tissue. The first jaw member 108 supports an anvil 111 and the second jaw member 110 releasably supports a staple cartridge 112. The buttress material 310 is mounted on the staple cartridge 112, as will be described. In order to secure the staples provided by the staple cartridge 112 to tissue and the buttress material 310, the anvil 111 is provided with longitudinally arranged rows of staple clinching or forming pockets (not shown). It is envisioned that the tool assembly 107 may be coupled to a mechanical or motorized handle, and the staple cartridge 112 may be removable and replaceable. It is also envisioned that the reload 106 may be part of a robotic surgical system.

With continued reference to FIG. 1 , the surgical stapling device 200 includes a stationary grip 222 and a rotation knob assembly 234. Buttons 26 a, 26 b on the stationary grip 222 of the handle 202 allow for actuation of the tool assembly 107. When the button 26 a is pressed, the tool assembly 107 is transitioned from the open configuration to the closed configuration and subsequently actuates the surgical stapling device 200 to apply lines of staples to tissue. When the button 26 b is pressed, a firing mechanism of the surgical stapling device 200 is retracted and the tool assembly 107 is transitioned from the closed configuration to the open configuration. In order to provide proper orientation of the tool assembly 107 relative to tissue to be stapled, the surgical stapling device 200 is additionally provided with the rotation knob assembly 234 mounted on the handle 202. Rotation of the rotation knob assembly 234 about a longitudinal axis “A-A” of the surgical stapling device 200 rotates the tool assembly 107 about the longitudinal axis “A-A.” The surgical stapling device 200 is illustrated as an electrically powered stapling device including the electrically powered handle 202 that may support one or more batteries (not shown). Examples of electrically powered surgical stapling devices can be found in U.S. Pat. Nos. 9,055,943 and 9,023,014. In addition, reference may be made to U.S. Pat. No. 9,717,498, the entire contents of which is incorporated herein by reference, for a detailed discussion of the construction and operation of the surgical stapling device 200.

FIGS. 3-5 illustrate the buttress material 310 for use with the surgical stapling device 200. The buttress material 310 is detachably secured to the tool assembly 107 of the surgical stapling device 200 to be in registration with the anvil 111 of the first jaw member 108 and the staple cartridge 112 of the second jaw member 110. The buttress material 310 is configured to reinforce and seal staple lines applied to tissue by the surgical stapling device 200. The buttress material 310 includes proximal and distal portions 310 a, 310 b that are detachably securable to the staple cartridge 112. In particular, the proximal portion 310 a includes proximal protrusions 311 that are spaced part. The proximal protrusions 311 extend laterally outwards from respective lateral sides of an elongate body 330 of the buttress material 310. Each proximal protrusion 311 defines a proximal bore 312 a. The proximal bores 312 a releasably receive respective proximal pegs 607 (FIG. 6 ) of a loading assembly 600. The proximal portion 310 a further defines a proximal slot 315 a that is configured to receive proximal hooks 510 (FIG. 6 ) and a notch 317 that is configured to receive a knife member (not shown) of the tool assembly 107. In an aspect, the proximal slot 315 a is substantially orthogonal to the longitudinal axis “A-A” (FIG. 1 ) of the surgical stapling device 200, and the notch 317 is centrally defined to be aligned with a knife channel 105 of the staple cartridge 112. The distal portion 310 b of the buttress material 310 includes distal protrusions 315 that are laterally spaced part. Each distal protrusion 315 extends laterally outwards from the corresponding lateral side of the elongate body 330 of the buttress material 310. Further, each distal protrusion 315 defines a distal bore 312 b that is dimensioned to releasably receive a corresponding distal peg 609 (FIG. 6 , only one shown) of the loading assembly 600. In another aspect, the buttress material 310 may be formed of an elastic material such that when the proximal and distal portions 310 a, 310 b of the buttress material 310 are releasably secured to the retention assembly 550 (FIG. 6 ) of the staple cartridge 112, the buttress material 310 is in tension to enhance securement with the staple cartridge 112.

The buttress material 310 is detachably securable to the tool assembly 107. To this end, the staple cartridge 112 includes the retention assembly 550 (FIG. 6 ) which is configured to releasably support the buttress material 310 on the buttress mounting surface 119 of the staple cartridge 112. FIGS. 6-9 illustrate the retention assembly 550 including proximal hooks 510 that are disposed in respective proximal slots 1205 defined in a proximal portion 112 a of the staple cartridge 112 and distal hooks 520 that are disposed in respective distal slots 1209 defined in a distal portion 112 b of the staple cartridge 112. The staple cartridge 112 includes a plurality of tabs 530 that are disposed on lateral sides 1208 of the staple cartridge 112 to align the loading assembly 600 supporting the buttress material 310 between the tabs 530.

FIG. 6 illustrates the proximal hooks 510 of the retention assembly 550 that are laterally spaced apart and disposed within the respective proximal slots 1205 of the staple cartridge 112. In particular, each proximal hook 510 defines proximal and distal gaps 515, 517 with inner walls of the staple cartridge 112 that define the proximal slot 1205 as shown in FIG. 8 . The proximal slots 1205 receive a portion of the buttress material 310 and/or the loading assembly 600, as will be described. In an aspect, the proximal hooks 510 may be positioned flush with or beneath the buttress mounting surface 119 of the staple cartridge 112. The proximal hooks 510 may be formed of an elastic material to enable flexing of the proximal hooks 510, in, e.g., an axial direction.

FIG. 6 further illustrates the distal hooks 520 that are laterally spaced apart and are disposed within the respective distal slots 1209 of the staple cartridge 112. In particular, each distal hook 520 defines proximal and distal gaps 525, 527 (FIG. 9 ) with the inner walls that define the distal slot 1209 to receive a portion of the buttress material 310 and/or the loading assembly 600, as will be described. In an aspect, the distal hooks 520 may be positioned flush with or beneath a buttress mounting surface 119 of the staple cartridge 112. The distal hooks 520 may be formed of an elastic material to enable flexing of the distal hooks 520 in, e.g., an axial direction. In an aspect, the proximal and distal hooks 510, 520 may be monolithically formed or molded on to the staple cartridge 112 as a single construct.

FIGS. 10 and 11 illustrate the loading assembly 600 that may be utilized in conjunction with the buttress material 310 to facilitate mounting of the buttress material 310 on the staple cartridge 112 (FIG. 7 ). In particular, the loading assembly 600 includes an elongate body 602, proximal protrusions 610 in a proximal portion 600 a of the loading assembly 600, and distal protrusions 620 in a distal portion 600 b of the loading assembly 600. The proximal and distal protrusions 610, 620 extend laterally outwards from the elongate body 602. The proximal portion 600 a defines cutouts 612 in lateral sides 613 of the elongate body 602. The cutouts 612 are configured to receive the tabs 530 (FIG. 8 ) of the staple cartridge 112 to facilitate alignment of the loading assembly 600 with the staple cartridge 112. In an aspect, the cutouts 612 are positioned distal of the proximal protrusions 610. The distal portion 600 b of the loading assembly 600 includes a guide 628 that is configured to be received in the knife channel 105 (FIG. 6 ) of the staple cartridge 112 to further facilitate alignment of the loading assembly 600 to the staple cartridge 112.

Each of the proximal protrusions 610 includes a proximal peg 607 that is configured to be received in the corresponding proximal bore 312 a of the buttress material 310, as shown in FIG. 11 . The proximal portion 600 a of the loading assembly 600 further includes proximal cups 615 that are configured to receive a portion of respective proximal hooks 510 (FIG. 6 ) of the retention assembly 550 of the staple cartridge 112. For example, portions of each proximal cup 615 are received in the proximal and distal gaps 515, 517 (FIG. 8 ) defined between the corresponding proximal hook 510 and the inner walls that define the proximal slot 1205. In an aspect, each proximal cup 615 may have a square or rectangular shape. In another aspect, each proximal cup 516 may have a circular shape. The proximal cups 615 are disposed interposed between the proximal protrusions 610.

As shown in FIGS. 10 and 11 , each distal protrusion 620 has the distal peg 609 that is configured to be received in the corresponding distal bore 312 b of the buttress material 310. The distal portion 600 b of the loading assembly 600 further includes distal cups 617 that are configured to receive a portion of the respective distal hooks 520 (FIG. 9 ) of the retention assembly 550 of the staple cartridge 112. For example, portions of each distal cup 617 are received in the proximal and distal gaps 525, 527 (FIG. 9 ) defined between the corresponding distal hook 520 and the inner walls of the staple cartridge 112 that define the corresponding distal slot 1209. In an aspect, each distal cup 617 may have a square or rectangular shape. In another aspect, the distal cups 617 may have a circular shape. The distal cups 617 are interposed between the distal protrusions 620. FIG. 11 illustrates the buttress material 310 releasably supported on the loading assembly 600. The proximal pegs 607 extend through the proximal bores 312 a of the buttress material 310, and the distal pegs 609 extend through the distal bores 312 b of the buttress material 310 such that the proximal and distal cups 615, 617 of the loading assembly 600 are in registration with the respective proximal and distal slots 315 a, 315 b of the buttress material 310. The proximal and distal pegs 607, 609 of the loading assembly 600 may engage the buttress material 310 via friction or interference fit. In an aspect, the loading assembly 600 further includes contact pads 614 (FIG. 10 ) that are disposed about the distal and proximal pegs 607, 609. The contact pads 614 contact the buttress material 310. The contact pads 614 may be formed of, e.g., gel or polymeric material, to reduce stress around the proximal and distal bores 312 a, 312 b of the buttress material 310 when the loading assembly 600 supporting the buttress material 310 is pressed against the staple cartridge 112, as described below.

In use, the buttress material 310 is first mounted on the loading assembly 600. The loading assembly 600 is placed on the staple cartridge 112 such that the buttress material 310 faces the buttress mounting surface 119 of the staple cartridge 112. The alignment of the loading assembly 600 to the staple cartridge 112 is achieved through the placement of the guide 628 in the knife channel 105 (FIG. 6 ) of the staple cartridge 112 and the placement of the tabs 530 of the staple cartridge 112 in the cutouts 612 defined in the proximal portion 600 a of the loading assembly 600. At this time, the proximal and distal cups 615, 617 of the loading assembly 600 are disposed on the buttress material 310 that is disposed on the buttress mounting surface 119, as best shown in FIG. 13 . As the loading assembly 600 is further pushed towards the staple cartridge 112 in the direction of arrows “D” (FIG. 4 ), each proximal cup 615 is pushed into the corresponding proximal slot 1205 of the staple cartridge 112 such that a portion of the buttress material 310 is placed in the proximal gap 515 (FIG. 8 ) and releasably secured to the staple cartridge 112 by the proximal hook 510. In addition, each distal cup 617 is pushed into the corresponding distal slot 1209 of the staple cartridge 112 such that a portion of the buttress material 310 is placed in the distal gap 527 (FIG. 9 ) of the staple cartridge 112 and releasably secured to the staple cartridge 112 by the distal hook 520, as best shown in FIG. 14 . The staple cartridge 112 having the buttress material 310 mounted thereon may now be supported on the second jaw 110 (FIG. 3 ) of the tool assembly 107 for stapling and severing of tissue.

It is further contemplated that the buttress material 310 may be made from any biocompatible natural or synthetic material. The material from which the buttress material 310 is formed may be bioabsorbable or non-bioabsorbable. It should be understood that any combination of natural, synthetic, bioabsorbable and non-bioabsorbable materials may be used to form the buttress material 310.

Some non-limiting examples of materials from which the buttress material 310 may be made include but are not limited to poly(lactic acid), poly (glycolic acid), poly (hydroxybutyrate), poly (phosphazine), polyesters, polyethylene glycols, polyethylene oxides, polyacrylamides, polyhydroxyethylmethylacrylate, polyvinylpyrrolidone, polyvinyl alcohols, polyacrylic acid, polyacetate, polycaprolactone, polypropylene, aliphatic polyesters, glycerols, poly(amino acids), copoly (ether-esters), polyalkylene oxalates, polyamides, poly (iminocarbonates), polyalkylene oxalates, polyoxaesters, polyorthoesters, polyphosphazenes and copolymers, block copolymers, homopolymers, blends and combinations thereof.

In aspects, natural biological polymers are used in forming the buttress material 310. Suitable natural biological polymers include, but are not limited to, collagen, gelatin, fibrin, fibrinogen, elastin, keratin, albumin, hydroxyethyl cellulose, cellulose, hydroxypropyl cellulose, carboxyethyl cellulose, chitan, chitosan, and combinations thereof. In addition, the natural biological polymers may be combined with any of the other polymeric materials described herein to produce the buttress material 310.

The buttress material 310 may be porous or non-porous, or combinations of porous and non-porous layers. Where the buttress material 310 is non-porous, the buttress material 310 may retard or inhibit tissue ingrowth from surrounding tissues thereby acting as an adhesion barrier and inhibiting the formation of unwanted scar tissue. Thus, in aspects, the buttress material 310 possesses anti-adhesion properties. Techniques for forming non-porous layers from such materials are within the purview of those skilled in the art and include, for example, casting, molding, and the like.

In aspects, the buttress material 310 is porous and possesses hemostatic properties. Where the buttress material 310 is porous, it has openings or pores over at least a portion of a surface thereof. Suitable materials for forming the porous layer include, but are not limited to foams (e.g., open or closed cell foams). In aspects, the pores may be in sufficient number and size so as to interconnect across the entire thickness of the porous layer. In other aspects, the pores do not interconnect across the entire thickness of the porous layer. In yet other aspects, the pores do not extend across the entire thickness of the porous layer, but rather are present at a portion of the surface thereof. In aspects, the openings or pores are located on a portion of the surface of the porous layer, with other portions of the porous layer having a non-porous texture. Those skilled in the art reading the disclosure will envision other pore distribution patterns and configurations for the porous layer.

Where the buttress material 310 is porous, the pores may be formed using any method suitable to forming a foam or sponge including, but not limited to the lyophilization or freeze-drying of a composition. Suitable techniques for making foams are within the purview of those skilled in the art. Porous buttress material 310 can be at least 0.2 cm thick, in aspects from about 0.3 to about 1.5 cm thick. Porous buttress material 310 can have a density of not more than about 75 mg/cm² and, in aspects below about 20 mg/cm². The size of the pores in the porous buttress material 310 can be from about 20 μm to about 300 μm, and in certain aspects from about 100 μm to about 200 μm.

The buttress material 310 may also include a reinforcement member. The reinforcement member may be associated with a porous or non-porous layer or may be positioned between a non-porous layer and a porous layer of the buttress material 310. Alternatively, the reinforcement member may be positioned entirely within one or more of the individual layers (e.g., embedded within the porous layer, the non-porous layer, or both) of the buttress material 310. It is also envisioned that the reinforcement member may be positioned at the surface of one of the layers making up the buttress material 310 and, in aspects, may be positioned at an exterior surface of the buttress material 310.

Some suitable non-limiting examples of reinforcement members include fabrics, meshes, monofilaments, multifilament braids, chopped fibers (sometimes referred to in the art as staple fibers) and combinations thereof. Where the reinforcement member is a mesh, it may be prepared using any technique known to those skilled in the art, such as knitting, weaving, tatting, knipling, or the like. Where monofilaments or multifilament braids are used as the reinforcement member, the monofilaments or multifilament braids may be oriented in any desired manner. For example, the monofilaments or multifilament braids may be randomly positioned with respect to each other within the buttress material 310. As another example, the monofilaments or multifilament braids may be oriented in a common direction within the buttress material 310. Where chopped fibers are used as the reinforcement member, the chopped fibers may be oriented in any desired manner. For example, the chopped fibers may be randomly oriented or may be oriented in a common direction. The chopped fibers can thus form a non-woven material, such as a mat or a felt. The chopped fibers may be joined together (e.g., by heat fusing) or they may be unattached to each other. The chopped fibers may be of any suitable length. For example, the chopped fibers may be from 0.1 mm to 100 mm in length, and in some aspects, 0.4 mm to 50 mm in length. In an aspect, the buttress material 310 has randomly oriented chopped fibers that have not been previously fused together and are embedded within in the buttress material 310.

It is envisioned that the reinforcement member may be formed from any bioabsorbable, non-bioabsorbable, natural, or synthetic material previously described herein and combinations thereof. Where monofilaments or multifilament braids are used as the reinforcement member, any commercially available suture material may advantageously be employed as the reinforcement member.

In aspects, at least one bioactive agent may be combined with the buttress material 310 and/or any of the individual components (the porous layer, the non-porous layer and/or the reinforcement member) used to construct the buttress material 310. In aspects, the buttress material 310 can also serve as a vehicle for delivery of the bioactive agent. The term “bioactive agent”, as used herein, is used in its broadest sense and includes any substance or mixture of substances that have clinical use. Consequently, bioactive agents may or may not have pharmacological activity per se, e.g., a dye, or fragrance. Alternatively, a bioactive agent could be any agent which provides a therapeutic or prophylactic effect such as a compound that affects or participates in tissue growth, cell growth, or cell differentiation.

Examples of classes of bioactive agents which may be utilized in accordance with the disclosure include anti-adhesives, antimicrobials, analgesics, antipyretics, anesthetics, antiepileptics, antihistamines, anti-inflammatories, cardiovascular drugs, diagnostic agents, sympathomimetics, cholinomimetics, antimuscarinics, antispasmodics, hormones, growth factors, muscle relaxants, adrenergic neuron blockers, antineoplastics, immunogenic agents, immunosuppressants, gastrointestinal drugs, diuretics, steroids, lipids, lipopolysaccharides, polysaccharides, and enzymes. It is also intended that combinations of bioactive agents may be used.

Anti-adhesive or anti-adhesion agents can be used to inhibit adhesions from forming between the buttress material 310 and the surrounding tissues opposite the target tissue. Some examples of these agents include, but are not limited to poly (vinyl pyrrolidone), carboxymethyl cellulose, hyaluronic acid, polyethylene oxide, poly vinyl alcohols and combinations thereof.

Suitable antimicrobial agents which may be included as a bioactive agent in the buttress material 310 of the disclosure include triclosan, also known as 2,4,4′-trichloro-2′-hydroxydiphenyl ether, chlorhexidine and its salts, including chlorhexidine acetate, chlorhexidine gluconate, chlorhexidine hydrochloride, and chlorhexidine sulfate, silver and its salts, including silver acetate, silver benzoate, silver carbonate, silver citrate, silver iodate, silver iodide, silver lactate, silver laurate, silver nitrate, silver oxide, silver palmitate, silver protein, and silver sulfadiazine, polymyxin, tetracycline, aminoglycosides, such as tobramycin and gentamicin, rifampicin, bacitracin, neomycin, chloramphenicol, miconazole, quinolones such as oxolinic acid, norfloxacin, nalidixic acid, pefloxacin, enoxacin and ciprofloxacin, penicillins such as oxacillin and pipracil, nonoxynol 9, fusidic acid, cephalosporins, and combinations thereof. In addition, antimicrobial proteins and peptides such as bovine lactoferrin and lactoferricin B may be included as a bioactive agent in the bioactive coating of the disclosure.

Other bioactive agents which may be included as a bioactive agent in the buttress material 310 in accordance with the disclosure include: local anesthetics; non-steroidal antifertility agents; parasympathomimetic agents; psychotherapeutic agents; tranquilizers; decongestants; sedative hypnotics; steroids; sulfonamides; sympathomimetic agents; vaccines; vitamins; antimalarials; anti-migraine agents; anti-parkinson agents such as L-dopa; anti-spasmodics; anticholinergic agents (e.g. oxybutynin); antitussives; bronchodilators; cardiovascular agents such as coronary vasodilators and nitroglycerin; alkaloids; analgesics; narcotics such as codeine, dihydrocodeinone, meperidine, morphine and the like; non-narcotics such as salicylates, aspirin, acetaminophen, d-propoxyphene and the like; opioid receptor antagonists, such as naltrexone and naloxone; anti-cancer agents; anti-convulsants; anti-emetics; antihistamines; anti-inflammatory agents such as hormonal agents, hydrocortisone, prednisolone, prednisone, non-hormonal agents, allopurinol, indomethacin, phenylbutazone and the like; prostaglandins and cytotoxic drugs; estrogens; antibacterials; antibiotics; anti-fungals; anti-viral s; anticoagulants; anticonvulsants; antidepressants; antihistamines; and immunological agents.

Other examples of suitable bioactive agents which may be included in the coating composition include viruses and cells, peptides, polypeptides and proteins, analogs, muteins, and active fragments thereof, such as immunoglobulins, antibodies, cytokines (e.g. lymphokines, monokines, chemokines), blood clotting factors, hemopoietic factors, interleukins (IL-2, IL-3, IL-4, IL-6), interferons (β-IFN, (α-IFN and γ-IFN), erythropoietin, nucleases, tumor necrosis factor, colony stimulating factors (e.g., GCSF, GM-CSF, MCSF), insulin, anti-tumor agents and tumor suppressors, blood proteins, gonadotropins (e.g., FSH, LH, CG, etc.), hormones and hormone analogs (e.g., growth hormone), vaccines (e.g., tumoral, bacterial and viral antigens); somatostatin; antigens; blood coagulation factors; growth factors (e.g., nerve growth factor, insulin-like growth factor); protein inhibitors, protein antagonists, and protein agonists; nucleic acids, such as antisense molecules, DNA and RNA; oligonucleotides; polynucleotides; and ribozymes.

While the disclosure has been shown in the drawings, it is not intended that the disclosure be limited thereto, as it is intended that the disclosure be as broad in scope as the art will allow and that the specification be read likewise. Therefore, the above description should not be construed as limiting, but merely as exemplifications. Those skilled in the art will envision other modifications within the scope and spirit of the claims appended hereto. 

What is claimed is:
 1. A surgical kit comprising: a surgical stapling device including: a tool assembly including first and second jaw members that are transitionable between open and closed configurations, the first jaw member supporting a staple cartridge that includes a retention assembly and defines proximal and distal slots, the retention assembly including: a proximal hook disposed within the proximal slot of the staple cartridge; and a distal hook disposed within the distal slot of the staple cartridge; a buttress material including an elongate body having proximal and distal portions, proximal protrusions extending laterally outwards from the proximal portion of the elongate body, and distal protrusions extending laterally outwards from the distal portion of the elongate body, the proximal protrusions defining respective proximal bores, the distal protrusions defining respective distal bores, the buttress material defining a proximal slot interposed between the proximal bores and a distal slot interposed between the distal bores; and a loading assembly including: proximal wings that are laterally spaced apart, each of the proximal wings including a proximal peg configured to be received through a corresponding one of the proximal bores of the buttress material; distal wings that are laterally spaced apart, each of the distal wings including a distal peg configured to be received through a corresponding one of the distal bores of the buttress material; a proximal cup configured to receive a portion of the proximal hook of the staple cartridge and engage a first portion of the buttress material to position the first portion of the buttress material in the proximal slot of the staple cartridge to be releasably secured to the proximal hook; and a distal cup configured to receive a portion of the distal hook of the staple cartridge and engage a second portion of the buttress material to position the second portion of the buttress material in the distal slot of the staple cartridge to be releasably secured to the distal hook.
 2. The surgical kit according to claim 1, wherein the loading assembly further includes a contact pad disposed about a portion of one of the proximal and distal pegs of the loading assembly.
 3. The surgical kit according to claim 1, wherein the proximal portion of the loading assembly defines cutouts on lateral sides of the loading assembly.
 4. The surgical kit according to claim 3, wherein the staple cartridge includes tabs received in the respective cutouts of the loading assembly.
 5. The surgical kit according to claim 1, wherein the distal portion of the loading assembly has a guide and the staple cartridge defines a knife channel, the guide configured to be received in the knife channel of the staple cartridge.
 6. The surgical kit according to claim 1, wherein the proximal and distal pegs of the loading assembly is configured to support the buttress material by friction or interference fit.
 7. The surgical kit according to claim 1, wherein the proximal or distal cups have a non-circular cross-section.
 8. The surgical kit according to claim 1, wherein the proximal cup is interposed between the proximal pegs.
 9. The surgical kit according to claim 1, wherein the proximal or distal hooks are formed of an elastic material to enable axial flexing of the proximal or distal hooks.
 10. The surgical kit according to claim 1, wherein the buttress material is formed of an elastic material that is placed in tension when the buttress material is secured to the staple cartridge.
 11. The surgical kit according to claim 1, wherein the proximal slot of the buttress material is in registration with the proximal cup when the buttress material is mounted on the loading assembly.
 12. A buttress assembly for use with a surgical stapling device comprising: a buttress material including proximal and distal portions, the proximal portion defining proximal bores laterally spaced apart and a proximal slot interposed between the proximal bores, the distal portion defining distal bores laterally spaced apart and a distal slot interposed between the distal bores; and a loading assembly including: proximal wings that are laterally spaced apart, each of the proximal wings including a proximal peg configured to be received in a corresponding one of the proximal bores of the buttress material; distal wings that are laterally spaced apart, each of the distal wings including a distal peg configured to be received in a corresponding one of the distal bores of the buttress material; a proximal cup interposed between the proximal pegs and configured to engage a first portion of the buttress material; and a distal cup interposed between the distal pegs and configured to engage a second portion of the buttress material, wherein when the proximal pegs of the loading assembly are received in the proximal bores of the buttress material, the proximal cup is in registration with the proximal slot of the buttress material, and wherein when the distal pegs of the loading assembly are received in the distal bores of the buttress material, the distal cup is in registration with the distal slot of the buttress material.
 13. The buttress assembly according to claim 12, wherein the loading assembly has opposing cutouts on lateral sides of the loading assembly.
 14. The buttress assembly according to claim 12, wherein a proximal end of the buttress material has a notch.
 15. The buttress assembly according to claim 12, wherein the distal portion of the loading assembly has a guide extending along a length of the loading assembly.
 16. The buttress assembly according to claim 15, wherein the guide of the loading assembly is distal of the distal pegs.
 17. The buttress assembly according to claim 12, wherein the loading assembly is symmetric about a central longitudinal axis.
 18. The buttress assembly according to claim 12, wherein the buttress material is bioabsorbable. 